Cat. No. / ID: Not Applicable
Proteinase K is a subtilisin-related serine protease derived from the Parengyodontium album (Tritirachium album) that is active under a wide range of reaction conditions, including elevated temperatures and the presence of Sodium Dodecyl Sulfate (SDS).
It is a broad-spectrum endopeptidase with a very high specific activity allowing highly effective digestion of proteins, including DNases and RNases, during nucleic acid preparations without compromising the integrity of isolated DNA or RNA.
The enzyme is expressed in Pichia pastoris, and undergoes extensive purification to yield the highest quality product. An additional purification technology significantly increases solubility (2.5 fold), increases specific activity, and produces remarkable purity with DNA content ≤0.1 pg/mg for Proteinase K Ultrapure.
Proteinase K is free of exonucleases, endonucleases, and ribonucleases.
One unit of Proteinase K hydrolyzes urea-denatured hemoglobin producing the color equivalent of 1 μmol tyrosine per 1 minute at 37°C and pH 7.5 (Folin & Ciocalteu’s method), 1 U = 1 mAnsonU.
|Assay||Proteinase K Powder and Solution Specification||Proteinase K Ultrapure Specification|
|Solubility in water||≥20 mg/mL||≥50 mg/mL|
|Activity||≥30 U/mg lyophilizate
≥40 U/mg protein
≥800 U/mL liquid
|≥35 U/mg lyophilizate
≥45 U/mg protein
|DNA content||≤10 pg/mg
|Single-stranded exonuclease||Not detected||Not detected|
|Double-stranded exonuclease||Not detected||Not detected|
|Double-stranded endonuclease||Not detected||Not detected|
Proteinase K is a recombinant Parengyodontium album (Tritirachium album) 28.9 kDa broad-spectrum serine protease expressed in Komagataella phaffii (Pichia pastoris) used for protein digestion and contamination removal during nucleic acid preparation. It cleaves the peptide bond adjacent to the carboxyl group of aliphatic, aromatic, and other hydrophobic amino acids. Because of its broad specificity and high stability at a wide range of pH and temperature, Proteinase K is routinely used in numerous molecular biology applications such as the isolation of genomic, plasmid, and high molecular weight DNA, RNA, and in inactivation of RNases and DNases. It is also used for effective digestion of structural proteins, chromatins, and inactivation of nucleases and RNases.
High-quality sample preparation is an essential step before the actual molecular analysis of the genetic material. This procedure includes multiple stages such as sample isolation, purification, and concentration of the target product, where Proteinase K plays an important role. Despite various reagents used in the process, the initial focus should be on Proteinase K, which certified quality assures high purity of tested nucleic acids.
Protein concentration was determined by measuring absorbance at 280 nm.
The presence of exonuclease was determined by gel electrophoresis of 1 μg of HindIII-digested λ DNA with 50 μg of Proteinase K incubated for 16 hours at 37°C.
The presence of endonuclease was determined by gel electrophoresis of 1 μg pUC19 DNA with 40 μg of Proteinase K incubated for 16 hours at 37°C.
The presence of RNase activity was determined by gel electrophoresis of 2 µg rRNA from E. coli with 20 μg of Proteinase K incubated for 4 hours at 37°C.
This product is available for molecular biology applications such as: